Variant report

Variant	rs17040169
Chromosome Location	chr2:50425302-50425303
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10490233	0.86[CHB][hapmap];0.96[JPT][hapmap];0.91[ASN][1000 genomes]
rs10490240	0.92[CEU][hapmap]
rs11125290	1.00[CEU][hapmap]
rs11125291	1.00[CEU][hapmap];0.84[AMR][1000 genomes]
rs11125292	1.00[CEU][hapmap];0.84[AMR][1000 genomes]
rs11125294	1.00[CEU][hapmap];0.84[AMR][1000 genomes]
rs11125295	1.00[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap]
rs11125296	0.93[CEU][hapmap];0.90[CHB][hapmap];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11888330	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11896556	0.93[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap]
rs11900502	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12466807	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12468151	0.83[AMR][1000 genomes]
rs12468252	1.00[CEU][hapmap];0.83[AMR][1000 genomes]
rs12468282	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12468396	0.83[AMR][1000 genomes]
rs12468477	1.00[CEU][hapmap]
rs12470518	0.85[CHB][hapmap]
rs12475100	0.88[CEU][hapmap];0.85[CHB][hapmap];0.83[JPT][hapmap]
rs12478603	1.00[CHB][hapmap];0.92[JPT][hapmap];0.99[ASN][1000 genomes]
rs12613266	0.81[AMR][1000 genomes]
rs12613363	0.80[CHB][hapmap]
rs12622844	1.00[CEU][hapmap];0.81[AMR][1000 genomes]
rs1377238	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap]
rs1421573	0.93[CEU][hapmap]
rs1452769	1.00[CEU][hapmap];0.84[CHB][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1452770	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1452771	1.00[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1452773	0.80[CEU][hapmap];0.85[CHB][hapmap]
rs1517827	0.80[AMR][1000 genomes]
rs1563019	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1563020	0.88[CEU][hapmap]
rs1563028	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap]
rs1584763	1.00[CEU][hapmap];0.82[AMR][1000 genomes]
rs17039764	0.81[CHB][hapmap]
rs17039905	0.81[AMR][1000 genomes]
rs17039932	1.00[CEU][hapmap];0.81[AMR][1000 genomes]
rs17039940	1.00[CEU][hapmap];0.81[AMR][1000 genomes]
rs17039947	1.00[CEU][hapmap];0.83[AMR][1000 genomes]
rs17039976	1.00[CEU][hapmap]
rs17039979	1.00[CEU][hapmap]
rs17039985	1.00[CEU][hapmap];0.82[AMR][1000 genomes]
rs17040013	1.00[CEU][hapmap]
rs17040034	1.00[CEU][hapmap];0.81[CHB][hapmap];0.83[JPT][hapmap]
rs17040064	0.88[CEU][hapmap];0.81[CHB][hapmap];0.80[AMR][1000 genomes]
rs17040090	1.00[CEU][hapmap];0.85[CHB][hapmap];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17040117	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap]
rs17040123	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs17040138	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17040141	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17040147	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17040160	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17040207	0.91[JPT][hapmap]
rs17040210	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs17040235	1.00[JPT][hapmap]
rs2176872	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2218979	0.80[CHB][hapmap]
rs4971649	1.00[CEU][hapmap];0.81[AMR][1000 genomes]
rs4971650	1.00[CEU][hapmap]
rs4971652	1.00[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4971653	1.00[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4971654	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4971655	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4971656	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4971658	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4971659	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4971661	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60500567	0.89[AMR][1000 genomes]
rs6545149	0.81[CHB][hapmap]
rs6545155	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6712102	0.93[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap]
rs6712119	0.93[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs6712423	0.93[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs6731397	0.88[CEU][hapmap];0.81[CHB][hapmap]
rs72878157	0.81[AMR][1000 genomes]
rs72881242	0.80[AMR][1000 genomes]
rs73930305	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7599349	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7607863	1.00[CEU][hapmap]
rs962332	0.81[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3388948	chr2:50092667-50602681	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
2	esv3399511	chr2:50092687-50602651	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv932915	chr2:50306630-50628415	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv2756107	chr2:50307245-50440043	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv948833	chr2:50307245-50459077	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1002344	chr2:50326207-50518933	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv535692	chr2:50326207-50518933	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv492164	chr2:50399251-51029090	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv581839	chr2:50409803-50438701	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
10	nsv1000653	chr2:50417660-51083470	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv535693	chr2:50417660-51083470	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50420400-50426000	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr2:50423000-50425600	Enhancers	H1 Cell Line	embryonic stem cell
3	chr2:50423200-50425400	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr2:50423200-50426000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr2:50423400-50426000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr2:50424600-50426000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr2:50424800-50425800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr2:50425000-50425800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:50425000-50426000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr2:50425000-50426400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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